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Variant (rsID / SNP)

rs316003

SLC22A2

rs316003 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A2. Location: chromosome 6, position 160,645,832. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A2Not classified
Variant type
synonymous_variant
Chromosome / position
6:160645832
HGVS
NM_003058.4,c.1506G>A,p.Val502Val
Allele change
Synonymous_V502V

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.